Answer:
Suppression of Abl reduces the severity of abnormal axonal guidance in PTP mutants
Explanation:
Axon guidance is a neural development subfield relating to the mechanism by which neurons send out axons to meet their right targets.
ABL gene is a protooncogene that encodes a protein tyrosine kinase involved in a variety of cellular processes. PTPs are known to signal a number of cellular processes, including cell development, differentiation, mitotic cycle, and oncogenic transformation.
Suppression of Abl reduces the severity of abnormal axonal guidance in PTP mutants.
Answer:
Following are the two advantages of endoplasmic reticulum.
1) Endoplasmic reticulum is an organelle of the cell which is responsible for the production of protein for the cell. This protein is sent to the Golgi apparatus where it is modified and used by the cell where it is needed.
2) Endoplasmic reticulum also helps in the removal of toxic substances from the cell. If these toxic substances are not removed, it causes damage to the cell.
Ansa million. once you're staring at in ordinary terms one technology, it relatively is, all those fruit flies have been produced via 2 mum and dad, then the only plausible parental genotype that provide you a 50/50 ratio is that if the mummy is XwXw and the father is Xry... this gene is carried on the X chromosome, and w represents white eyes and r represents purple eyes. you are able to bypass forward and draw this out in case you like, even yet it provides 50% heterozygous women individuals (with purple eyes, provided that purple is dominant), and 50% white eyed men, who can in ordinary terms inherit Xw from their mom. The Y that they could inherit from the father could have not any effect on their eye shade. it relatively is comparable for women individuals, they are in a position to in ordinary terms inherit Xw from their mom and an Xr from their father, meaning they'll continually be heterozygous for the attention shade gene. 2. returned, set us the genotypes so which you will visualize it; we are going to say that this disease is carried on the X chrmsm (thats whats usually assumed), and the gene for customary creative and prescient is XB, yet for colorblindness its Xb. those are dominant/recessive to boot. So, if the girl is a provider, her genotype is XBXb, and if the male is colorblind, his genotype is XbY. in case you draw this out in a punett sq., you will get 25% heterozygous woman, 25% colorblind woman, 25% well-known male, and 25% colorblind male. so, there's a 50% risk that any baby they have would be colorblind, 50% risk if its a woman, or 50% risk if it relatively is male.wer:
Explanation:
A specific protein called a receptor
